Human cytomegalovirus infection and anti-receptor antibody
Human cytomegalovirus infection and anti-receptor antibody
批准号:
05670700
负责人:
ABE Toshiaki
金额:
$1.22万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1993
资助国家:
日本
项目状态:
已结题
起止时间:
1993 至 1994
中文摘要
在本研究中,我们发现先天性CMV感染患者的血清显示出针对硫酸化葡萄糖醛酸鞘糖脂(SGGL)的抗体滴度升高,SGGL含有单克隆抗体HN* 1反应性碳水化合物表位。SGPG在其nLc 4 * 的非还原端含有硫酸化葡萄糖醛酸,并且SGLPG具有类似的结构,但具有乳糖胺的额外单元。有趣的是,CMV感染患者血清中的抗体对SGLPG的反应性高于对SGPG的反应性,这种独特的特异性不同于其他HNK-1相关抗体。此外,抗硫苷脂和抗SG * 抗体均被硫苷脂缀合的辛基琼脂糖柱和肝素琼脂糖柱吸收,而CMV特异性IgG滴度不因抗硫酸化GL抗体的吸收而降低。结果表明,CMV感染可特异性地诱导抗硫酸盐抗体的产生,而这些抗体不同于CMV特异性抗体。纯化的HNK-1抗体可与HCMV阳性抗原和抗HNK-1抗体结合。用亲和层析法从病人血清中部分纯化的抗SGGL抗体也能与两种抗原结合,但其反应性低于抗HCMV抗体。这些结果表明,HNK-1表位的表达水平没有被HCMV感染改变,并且含有HNK-1表位的糖缀合物也存在于HCMV容许细胞中。此外,在病毒接种前用HCMV容许细胞预处理纯化的HNK-1抗体可抑制HCMV的空斑形成,表明宿主细胞中含有HNK-1糖表位的糖缀合物在HCMV感染过程中具有特殊作用。
英文摘要
In the present study we found that sera from patients with congenital CMV infection showed elevated titers* antibodies against sulfated glucuronyl glycosphingolipids (SGGL), which contain a monoclonal antibody HN* 1 reactive carbohydrate epitope. SGPG contains sulfated glucuronic acid on its non-reducing end of nLc4* and SGLPG has a similar structure but with an additional unit of lactosamine. Interesingly the antibodies* CMV infected patients'sera showed a higher reactivity to SGLPG than SGPG.This unique specificity * different from that of other HNK-1 related antibodies. Furthermore both anti-sulfatide and anti-SG* antibodies were absorbed with sulfatide-conjugated octyl-Sepharose column and heparin-Sepharose colur* whereas CMV specific IgG titer was not decreased by the absorption of anti-sulfated GL antibody. Th* results suggested that CMV infection might specifically induce production of antibodies against sulfated (* whereas these antibodies differed from CMV specific antibody.Then we studied whether the antibodies were produced against altered glycoconjugate patterns of host cell* a result of CMV infection. It was found that purified HNK-1 antibody bound to HCMV-positive and -negat* antigens. Anti-SGGL antibodies, which were partially purified from patient's sera by affinity chromatograp* also bound to both antigens, whereas the reactivity was lower than that of anti-HCMV antibodies. These res* indicate that a level of the HNK-1 epitope expression was not altered by HCMV infection and also t* glycoconjugates containing HNK-1 epitope were present in HCMV permissive cells. Furthermore, * pretreatment of the purified HNK-1 antibody with HCMV permissive cells prior to virus inoculation inhibi* plaque formation of HCMV,suggesting that the glycoconjugates containing HNK-1 carbohydrate epitope in* host cell have a special role in the process of HCMV infection.
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K.Ogawa-Goto etal: "Glycosphingolipids of human peripheral nervous system myelins isolated from cauda equina." J.Neurochem.61. 1398-1403 (1993)
K.Okawa-Goto 等人:“从马尾分离出的人类周围神经系统髓磷脂的糖鞘脂。”
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通讯作者:
K.Ogawa-Goto,et al.: "Antibodies against sulfated glycosphingolipids of peripheral nerve myelins detected in the patients with human cytomegalovirus infection." J.Neuroimmunol.55. 55-60 (1994)
K.Okawa-Goto 等人:“在人类巨细胞病毒感染患者中检测到周围神经髓磷脂硫酸化鞘糖脂的抗体。”
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作者:
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通讯作者:
Ogawa-Goto, K., Kubota, K.et al.: "Antibodies against sulfated glycosphingolipids of peripheral nerve myelins detected in the patients with human cytomegalovirus infection." J.Neuroimmunol. 55. 55-60 (1994)
Okawa-Goto, K.、Kubota, K.等人:“在人类巨细胞病毒感染患者中检测到周围神经髓磷脂硫酸化鞘糖脂的抗体。”
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作者:
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通讯作者:
Ogawa-Goto, K., Ohta, Y.et al.: "Glycosphingolipids of human pripheral nervous system myelins isolated from cauda equina." J.Neurochem. 61. 1398-1403 (1993)
Okawa-Goto, K.、Ohta, Y.等人:“从马尾分离出的人类周围神经系统髓磷脂的糖鞘脂。”
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通讯作者:
Intervention of retinal diseases using energy metabolism reprogramming
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批准号:20K21642
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项目类别:Grant-in-Aid for Challenging Research (Exploratory)
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-
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负责人:ABE Toshiaki
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依托单位:
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Transplantation study against ischemic retinal disease
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财政年份:1998
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依托单位:
Examination of phosducin gene
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项目类别:Grant-in-Aid for Scientific Research (C)
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财政年份:1996
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依托单位:
国内基金
海外基金
HNK-1抗原相关寡糖的合成及构效关系研究
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批准号:21702125
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项目类别:青年科学基金项目
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资助金额:25.0万元
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批准年份:2017
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负责人:彭鹏
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依托单位:
运动型胶质细胞HNK-1糖基蛋白对周围神经再生选择性的影响和作用机制
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批准号:31100782
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批准年份:2011
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负责人:王文进
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依托单位: